ClinVar Miner

Submissions for variant NM_002029.4(FPR1):c.289C>A (p.Leu97Met)

gnomAD frequency: 0.00362  dbSNP: rs78488639
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002233924 SCV000752041 benign Gingival disorder 2024-01-23 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV004717694 SCV005312207 benign not provided criteria provided, single submitter not provided
PreventionGenetics, part of Exact Sciences RCV003935753 SCV004749901 benign FPR1-related disorder 2019-12-16 no assertion criteria provided clinical testing This variant is classified as benign based on ACMG/AMP sequence variant interpretation guidelines (Richards et al. 2015 PMID: 25741868, with internal and published modifications).

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